Christer Halldén (Former)
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- 2023
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Mark
Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank
(
- Contribution to journal › Letter
- 2022
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Mark
Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults : A Population-Based Cohort Study
(
- Contribution to journal › Article
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Mark
Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults : A Population-Based Cohort Study
(
- Contribution to journal › Article
- 2021
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Mark
Droplet digital PCR and mile-post analysis for the detection of F8 int1h inversions
(
- Contribution to journal › Article
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Mark
Thrombotic Risk Determined by STAB 2 Variants in a Population-Based Cohort Study
(
- Contribution to journal › Letter
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Mark
Identification of F8 rearrangements in carrier and non-carrier mothers of haemophilia A patients
(
- Contribution to journal › Letter
- 2020
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Mark
Detection of F8 int22h inversions using digital droplet PCR and mile-post assays
(
- Contribution to journal › Article
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Mark
Detection of mosaics in hemophilia A by deep Ion Torrent sequencing and droplet digital PCR
(
- Contribution to journal › Article
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Mark
Genetic risk factors for venous thromboembolism
(
- Contribution to journal › Scientific review
- 2019
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Mark
Targeted re-sequencing of F8, F9 and VWF : Characterization of Ion Torrent data and clinical implications for mutation screening
(
- Contribution to journal › Article
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Mark
Next-Generation Sequencing of 17 Genes Associated with Venous Thromboembolism Reveals a Deficit of Non-Synonymous Variants in Procoagulant Genes
(
- Contribution to journal › Article
- 2018
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Mark
Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients
(
- Contribution to journal › Article
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Mark
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
(
- Contribution to journal › Article
- 2017
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Mark
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population
(
- Contribution to journal › Article
- 2016
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Mark
Origin of mutation in sporadic cases of severe haemophilia A in Sweden.
(
- Contribution to journal › Article
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Mark
Chronic rhinosinusitis patients show accumulation of genetic variants in PARS2
(
- Contribution to journal › Article
- 2014
-
Mark
Genetic Variation in KLK2 and KLK3 Is Associated with Concentrations of hK2 and PSA in Serum and Seminal Plasma in Young Men
(
- Contribution to journal › Article
- 2013
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Mark
Copy number variants in the kallikrein gene cluster.
(
- Contribution to journal › Article
- 2012
-
Mark
Evaluation of Multiple Risk-Associated Single Nucleotide Polymorphisms Versus Prostate-Specific Antigen at Baseline to Predict Prostate Cancer in Unscreened Men
(
- Contribution to journal › Article
-
Mark
Toll-like receptor gene polymorphisms are associated with allergic rhinitis: a case control study
(
- Contribution to journal › Article
-
Mark
Investigation of disease-associated factors in haemophilia A patients without detectable mutations.
(
- Contribution to journal › Article
- 2011
-
Mark
A large deletion identified in a Swedish family with type 1 VWD
(
- Contribution to journal › Letter
-
Mark
A Systematic Study of Gene Mutations in Urothelial Carcinoma; Inactivating Mutations in TSC2 and PIK3R1.
(
- Contribution to journal › Article
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Mark
Estrogen receptor alpha single nucleotide polymorphism modifies the risk of azoospermia in childhood cancer survivors
(
- Contribution to journal › Article
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Mark
Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease.
(
- Contribution to journal › Article
- 2010
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Mark
Polymorphisms at the Microseminoprotein-beta Locus Associated with Physiologic Variation in beta-Microseminoprotein and Prostate-Specific Antigen Levels
(
- Contribution to journal › Article
-
Mark
CLC- a novel susceptibility gene for allergic rhinitis?
(
- Contribution to journal › Article
-
Mark
Susceptibility Loci Associated with Prostate Cancer Progression and Mortality
(
- Contribution to journal › Article
-
Mark
Blood Biomarker Levels to Aid Discovery of Cancer-Related Single-Nucleotide Polymorphisms: Kallikreins and Prostate Cancer.
(
- Contribution to journal › Article
-
Mark
Effect of androgen deprivation therapy on the expression of prostate cancer biomarkers MSMB and MSMB-binding protein CRISP3.
(
- Contribution to journal › Article
-
Mark
Combined gene expression and genomic profiling define two intrinsic molecular subtypes of urothelial carcinoma and gene signatures for molecular grading and outcome.
(
- Contribution to journal › Article
- 2009
-
Mark
Permanent Genetic Resources added to Molecular Ecology Resources Database 1 May 2009-31 July 2009
(
- Contribution to journal › Article
-
Mark
Important research questions in allergy and related diseases: 3-chronic rhinosinusitis and nasal polyposis - a GA(2)LEN study
(
- Contribution to journal › Scientific review
-
Mark
A haplotype in the inducible T-cell tyrosine kinase is a risk factor for seasonal allergic rhinitis
(
- Contribution to journal › Article
-
Mark
Association between polymorphisms in the prostate-specific antigen (PSA) promoter and release of PSA.
(
- Contribution to journal › Article
- 2008
-
Mark
Distribution of von Willebrand factor levels in young women with and without bleeding symptoms. Influence of ABO blood group and promoter haplotypes
(
- Contribution to journal › Article
-
Mark
Comprehensive evaluation of genetic variation in S100A7 suggests an association with the occurrence of allergic rhinitis.
(
- Contribution to journal › Article
- 2007
-
Mark
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
(
- Contribution to journal › Article
-
Mark
The evolutionary history of the common chloroplast genome of Arabidopsis thaliana and A. suecica.
(
- Contribution to journal › Article
-
Mark
Evolution of chloroplast mononucleotide microsatellites in Arabidopsis thaliana
(
- Contribution to journal › Article
- 2006
-
Mark
A unique recent origin of the allotetraploid species Arabidopsis suecica: Evidence from nuclear DNA markers
(
- Contribution to journal › Article
-
Mark
A quality assessment survey of SNP genotyping laboratories
(
- Contribution to journal › Article
- 2005
-
Mark
Detecting Deletions in Families Affected by a Dominant Disease by Use of Marker Data.
(
- Contribution to journal › Article
-
Mark
Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype.
(
- Contribution to journal › Article
-
Mark
Large deletions of the PROS1 gene in a large fraction of mutationnegative patients with protein S deficiency
(
- Contribution to journal › Article
- 2004
-
Mark
Androgen receptor gene GGN and CAG polymorphisms among severely oligozoospermic and azoospermic Swedish men.
(
- Contribution to journal › Article
-
Mark
Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1.
(
- Contribution to journal › Article
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Mark
Mode of reproduction in Arabidopsis suecica
(
- Contribution to journal › Article
- 2003
-
Mark
Chloroplast DNA indicates a single origin of the allotetraploid Arabidopsis suecica.
(
- Contribution to journal › Article
-
Mark
The Moraxella catarrhalis immunoglobulin D-binding protein MID has conserved sequences and is regulated by a mechanism corresponding to phase variation.
(
- Contribution to journal › Article